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Metabolites of PAHs in bile were quantified by use of a modification of the method published by Kammann et al. [35].
CCR5 and HIV-1 copies in each sample were quantified by use of the obtained threshold values from the samples and the corresponding standard curve, constructed from multiple measurements of standards.
FA were quantified by use of Chromeleon® 6.8 Chromatography Software (Dionex, USA).
Active murine u-PA levels were quantified by use of a u-PA activity assay kit (Innovative Research, Michigan, USA), in accordance with the manufacturer's instructions.
Cell lysates were quantified by use of the Bradford assay and analysed for protein expression by applying 50 μg of protein extract from each lysate.
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Gel components were quantified by using partial least squares (PLS) calibration models of the PLS1 type.
Patient symptoms were quantified by using a disease-specific health-related quality of life questionnaire.
DCU plasma concentrations were quantified by using LC/MS/MS.
The bands were quantified by using the software ImageJ 1.32j.
Proteins were quantified by using Scion Image software.
Western blots were scanned and the bands were quantified by using NIH ImageJ software.
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